rs515726189
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs515726189(A;A) |
Make rs515726189(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 102224909 |
Gene | RRM2B |
is a | snp |
is | mentioned by |
dbSNP | rs515726189 |
dbSNP (classic) | rs515726189 |
ClinGen | rs515726189 |
ebi | rs515726189 |
HLI | rs515726189 |
Exac | rs515726189 |
Gnomad | rs515726189 |
Varsome | rs515726189 |
LitVar | rs515726189 |
Map | rs515726189 |
PheGenI | rs515726189 |
Biobank | rs515726189 |
1000 genomes | rs515726189 |
hgdp | rs515726189 |
ensembl | rs515726189 |
geneview | rs515726189 |
scholar | rs515726189 |
rs515726189 | |
pharmgkb | rs515726189 |
gwascentral | rs515726189 |
openSNP | rs515726189 |
23andMe | rs515726189 |
SNPshot | rs515726189 |
SNPdbe | rs515726189 |
MSV3d | rs515726189 |
GWAS Ctlg | rs515726189 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs515726189(A;A) |
Alt | rs515726189(A;A) |
Reference | Rs515726189(G;G) |
Significance | Pathogenic |
Disease | RRM2B-related mitochondrial disease |
Variation | info |
Gene | RRM2B |
CLNDBN | RRM2B-related mitochondrial disease |
Reversed | 0 |
HGVS | NC_000008.10:g.103237137G>A |
CLNSRC | ClinVar |
CLNACC | RCV000118997.2, |